Senior Director, Global Clinical Development (GI Oncology)
Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Key Responsibilities
Owns and drives clinical development strategy across given asset indications, aligned to overall asset strategy, Target Product Profile (TPP), and relevant disease area strategy.
May lead the Clinical Development Team(s) for given indication(s) depending on program structure.
Represents Clinical as the internal and external authority for the indication/disease area, including regulatory interactions and Business Development support.
Engages cross-functionally with internal leaders and partners with external investigators, key opinion leaders, and patient advocacy groups.
Presents clinical strategy, data, and risk assessments to governance bodies, health authorities, and senior leadership.
Leads a team of physicians and scientists in the design, execution, analysis, and interpretation of all clinical studies for respective indication(s).
Ensures studies meet regulatory, quality, medical, and access objectives and are aligned with target label indications.
Ensures high quality, timely delivery of innovative protocols and data packages for CSRs and Regulatory Filings; implements quality assurance plans.
Accountable for clinical content and data quality for CSRs, trial documents, regulatory submissions, briefing books, and publications.
Oversees trial progress, proactively identifies and mitigates risk, and provides regular status and risk updates to senior management.
Champions quality, compliance, and GCP adherence across all clinical activities, partnering with Development Operations and Compliance as needed.
Sets priorities aligned to program objectives and works with Clinical Asset leadership to ensure appropriate budget/resourcing.
Arrts, develops, and retains top clinical talent through effective leadership, mentoring, and training.
Fosters a culture of scientific excellence, collaboration, innovation, and accountability.
Qualifications & Experience
Advanced degree in Life Sciences required (PhD, PharmD, MS, RN, MD or related field, MD)
Deep clinical and therapeutic area expertise with advanced knowledge of drug development, competitive landscape, and health authority expectations.
8+ years of relevant experience, including leadership in the design and execution of multiple clinical trials.
Demonstrated success in people leadership and/or matrix leadership roles.
Compensation Overview
Cambridge Crossing: $273,900 - $331,907
Madison - Giralda - NJ - US: $244,560 - $296,352
Princeton - NJ - US: $244,560 - $296,352